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    • Exploring Senataxin -- Sen1p homology 

      Malone, Elizabeth A. (2010)
      Mutated SETX, a human gene encoding for the protein Senataxin, has been identified among patients with two different neurodegenerative disorders--ataxia-ocular apraxia 2 (AOA2) and amyotrophic lateral sclerosis 4 (ALS4). ...